Productive infection of both CD4+ and CD4- human cell lines with HIV-1, HIV-2 and SIVagm

AIDS. 1990 Jun;4(6):537-44. doi: 10.1097/00002030-199006000-00007.

Abstract

Human monolayer cells of various origins were shown to be susceptible to infection by HIV-1, HIV-2 and simian immunodeficiency virus obtained from African green monkeys (SIVagm). Immunoperoxidase staining revealed infection of 2-7% of the monolayer cells, although in order to achieve infection approximately 50-fold more virus was necessary than with CD4(+)-permissive lymphoma cells. No CD4-receptor antigen expression by fibroblastoid cells was detectable by immunofluorescence using several monoclonal antibodies (MAbs), although a low level of CD4-specific messenger RNA expression was revealed by Northern analysis (with the exception of Tera-1 and RD cells). Attempts to block viral infection by anti-CD4 MAbs indicated a CD4 receptor-mediated mechanism for all lines tested except RD cells. We conclude that a low level of CD4-receptor expression is sufficient to allow infection of fibroblastoid cells. The infectability of a CD4-negative cell line indicates a second pathway of cellular infection, possibly mediated by a cellular receptor distinct from the CD4 molecule.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acquired Immunodeficiency Syndrome / microbiology*
  • Animals
  • Antibodies, Monoclonal / immunology
  • Binding Sites
  • CD4 Antigens / genetics
  • CD4 Antigens / immunology
  • CD4-Positive T-Lymphocytes / microbiology*
  • Cell Line
  • HIV-1 / genetics
  • HIV-1 / immunology
  • HIV-1 / pathogenicity*
  • HIV-2 / genetics
  • HIV-2 / immunology
  • HIV-2 / pathogenicity*
  • Humans
  • Mice
  • Mice, Inbred Strains
  • RNA, Messenger / immunology
  • Receptors, Antigen, T-Cell / immunology
  • Retroviridae / genetics
  • Retroviridae / immunology*
  • Simian Immunodeficiency Virus / genetics
  • Simian Immunodeficiency Virus / immunology
  • Simian Immunodeficiency Virus / pathogenicity*
  • Tumor Cells, Cultured

Substances

  • Antibodies, Monoclonal
  • CD4 Antigens
  • RNA, Messenger
  • Receptors, Antigen, T-Cell